2009
DOI: 10.1097/aog.0b013e3181a9479e
|View full text |Cite
|
Sign up to set email alerts
|

Triple-Marker Prenatal Screening Program for Chromosomal Defects

Abstract: III.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
17
0

Year Published

2012
2012
2021
2021

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 47 publications
(17 citation statements)
references
References 16 publications
0
17
0
Order By: Relevance
“…Women who underwent screening in the second trimester only were not included in our cohort, because these results have been previously reported. 3,4 Screen-positive interpretation qualified women for follow-up services at a state-approved Prenatal Diagnostic Center. Follow-up services include genetic counseling and diagnostic services such as chorionic villus sampling, second-trimester ultrasonography, and amniocentesis.…”
Section: Methodsmentioning
confidence: 99%
See 2 more Smart Citations
“…Women who underwent screening in the second trimester only were not included in our cohort, because these results have been previously reported. 3,4 Screen-positive interpretation qualified women for follow-up services at a state-approved Prenatal Diagnostic Center. Follow-up services include genetic counseling and diagnostic services such as chorionic villus sampling, second-trimester ultrasonography, and amniocentesis.…”
Section: Methodsmentioning
confidence: 99%
“…3 All chromosomal abnormalities included in this study were diagnosed by karyotype. Registry ascertainment sources include physicians, cytogenetic laboratories, hospitals, and prenatal diagnostic centers.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…GDSP contracts with regional laboratories to analyse the serum biomarkers for gravid women who decide to participate. The laboratories use a uniform assay protocol that includes an automated analytical system [25,26].…”
Section: Methodsmentioning
confidence: 99%
“…1 Indications for amniocyte karyotyping are advanced maternal age, abnormal maternal serum screening results, abnormal prenatal ultrasound findings, and known family history of chromosomal anomalies or hereditary diseases. 2,3 In recent years, Taiwanese women have married later and become pregnant at older ages. After the implementation of national health insurance, antenatal care usage also increased.…”
Section: Introductionmentioning
confidence: 99%